A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067129



Internal ID18809660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35336133..35358408hg38UCSC Ensembl
Innerchr19:35827036..35849310hg19UCSC Ensembl
Innerchr19:40518876..40541150hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3822276
hg1922275
hg1822275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3566600
Samples
Known GenesCD22, FFAR1, MIR5196
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067129
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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